A bright single photon source: Strong coupling of a single molecule to a plasmonic nano-antenna cavity

Single photon emitters are quantum light sources that can enable a variety of quantum based technologies such as quantum information or quantum random number generation, among others. These single photon emitters can have their brightness increased by coupling to a plasmonic cavity. In this work, th...

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Detalles Bibliográficos
Autor: Izquierdo López, Raúl
Tipo de recurso: tesis de maestría
Fecha de publicación:2019
País:España
Institución:Universitat Politècnica de Catalunya (UPC)
Repositorio:UPCommons. Portal del coneixement obert de la UPC
Idioma:inglés
OAI Identifier:oai:upcommons.upc.edu:2117/168885
Acceso en línea:https://hdl.handle.net/2117/168885
Access Level:acceso abierto
Palabra clave:Nanophotonics
Antennas (Electronics)
Single molecule
single photon source
plasmonic cavity
coupling
Nanofotònica
Antenes (Electrònica)
Àrees temàtiques de la UPC::Enginyeria de la telecomunicació::Telecomunicació òptica::Fotònica
Descripción
Sumario:Single photon emitters are quantum light sources that can enable a variety of quantum based technologies such as quantum information or quantum random number generation, among others. These single photon emitters can have their brightness increased by coupling to a plasmonic cavity. In this work, this possibility is addressed by spin coating anthracene crystals hosting dibenzoterrylene (DBT) molecules on top of Au dipolar nanoantenna arrays. Thin anthracene crystals covering a big fraction of the nanoantenna arrays were achieved, on which confocal fluorescence microscopy and time correlated single photon counting have been used to characterize the emitters. A time gating based analysis has been used to separate the nanoantenna luminescence from the fluorescence of the DBT molecules, obtaining lifetime values from coupled and uncoupled molecules. A set of 149 coupled molecules and 158 uncoupled molecules was represented in a histogram, showing a distribution from whose mean values the lifetime of DBT molecules (t=4.37 ns) was acquired, as well as a mean lifetime reduction of 2.4 times and a maximum lifetime reduction of 7 times.